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The Sr. In-House CRA assists the Clinical Research Manager for one or more clinical studies. The Sr. In-House CRA assists with management of vendors such as CROs, Central Lab and other suppliers. The Sr. In-House CRA is responsible for matrix mananagement of functional area leads to meet study deliverables. The Sr. In-House CRA keeps aware of both internal and external business environments and th...
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Posted Tue 16th April
Clinical Research Associates (home based) - $5,000 sign on bonus! Multiple positions available We have exciting opportunities available to work within a fast paced environment for ICON Clinical Research, a leading global provider of outsourced clinical research/development services to the pharmaceutical, biotechnology and medical device industries. Working within a highly qualified team, our Clini...
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Posted Thu 25th April
Growing and well-respected biomedical (clinical, basic and applied) research firm has openings at USAMMDA. If you are passionate about research, and are looking for a firm that shares your passion, and provides competitive salaries with a strong benefits package, join the ClinicalRM team. We are currently seeking a Senior Clinical Research Associate for the Frederick, Maryland area. RESPONSIBILITI...
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Posted Tue 30th April
Clinical Research Associate This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Working within a highly qualified team our Clinical Research Associates (CRA’s) identify, select, initiate and close-out investigational sites for clinical studi...
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Posted Sat 4th May
Clinical Research Associate This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Working within a highly qualified team our Clinical Research Associates (CRA’s) identify, select, initiate and close-out investigational sites for clinical studi...
Full job description at Monster
Posted Sat 4th May
Clinical Research Associate This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Working within a highly qualified team our Clinical Research Associates (CRA’s) identify, select, initiate and close-out investigational sites for clinical studi...
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Posted Sat 4th May
The Clinical Research Associate (CRA) is responsible for performing any/all of the following tasks and responsibilities, as well as any other tasks deemed appropriate by the Supervisor: · Monitor activities at assigned clinical study sites to assure adherence to ICH GCPs, local regulatory requirements, Standard Operating Procedures (SOPs), Standard Guidelines (SGs), Instruction Manuals (IMs), stud...
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Posted Mon 6th May
The Clinical Research Associate (CRA) is responsible for performing any/all of the following tasks and responsibilities, as well as any other tasks deemed appropriate by the Supervisor: · Monitor activities at assigned clinical study sites to assure adherence to ICH GCPs, local regulatory requirements, Standard Operating Procedures (SOPs), Standard Guidelines (SGs), Instruction Manuals (IMs), stud...
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Posted Mon 6th May
Description of Work: Working with limited direction, is responsible for assisting in the coordination of clinical data collection, researching and analyzing technical data associated with clinical protocol testing and/or post market surveillance studies, and ensuring that site administration paper work is both complete and current. In addition, this position ensures appropriate monitoring of desig...
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Posted Wed 8th May
We’ve been engaged by our client to recruit their Sr. Clinical Research Associate. This position is responsible for assisting with the design and execution of high quality clinical trials to ensure the safety and performance of the company’s products. Coordinate the overall administration of clinical trials including study design, project tracking, CRO oversight, monitoring plans, review of monito...
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Posted Wed 8th May
. Exciting direct hire opportunity for a Full Time Clinical Research Associate in Pleasanton, CA! Responsibilities include: Works under general supervision, and participates in the design, planning, implementation and overall direction of clinical research projects; May co-ordinate the activities of relevant colleagues within the Company and investigators to ensure compliance with the overall scie...
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Posted Fri 17th May
Clinical Research Associate This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Working within a highly qualified team our Clinical Research Associates (CRA’s) identify, select, initiate and close-out investigational sites for clinical studi...
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Posted 3 days ago
CRA, Home-based, Regional, 1-2 protocols, 15 sites per month Are you a Clinical Research Associate and interested in an exciting new opportunity? ICON is a Global CRO who specializes in the therapeutic arena's; Oncology, Vaccines, Diabetes, and Transplants. They are growing quickly and currently looking for several CRAII and Sr.CRA's who work home-based and travel 65-75% of the time. This is a ful...
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Posted Yesterday
The Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and PPD Standard Operating Procedures. Conducts site visits to assess protocol and regulatory compliance and manages required documentation Responsible for ensuring that data will pass int...
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Posted Mon 6th May
Connexion Systems & Engineering, a Boston based IT and Engineering Solutions Company immediately seeks individuals with the following skills: Job# bh782 Clinical Research To oversee the conduct of clinical trials at assigned trial sites, within the agreed time scale, by regular monitoring. Once responsibility has been assigned, the CRA is the primary contact between the trial site and Sponsor. All...
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Posted Yesterday
About XBiotech XBiotech is a drug research & development center headquartered in Austin, Texas. Our Austin facility incorporates all critical operations including discovery, research and development, drug testing, product formulation, as well as, clinical-regulatory affairs. XBiotech is also a fully integrated biotech company. From pre-clinical models to clinical trial execution, from discovery to...
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Posted Mon 6th May
SUMMARY Able to work independently to implement and monitor clinical studies at participating study sites according to FDA’s Code of Federal Regulations (CFR), Good Clinical Practices (GCP), and ICH Guidelines. Works with Clinical Affairs management to plan and execute the design and conduct of Dexcom-sponsored (including In-House studies). Responsible for overall study planning and ensuring that ...
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Posted Tue 7th May
Position Description: We are currently seeking an Associate Director of Clinical Affairs is responsible, in collaboration with the clinical Research Project Managers, for development and execution of the clinical research studies. The Associate Director will act in a supervisory capacity to the clinical Research Project Managers but will be jointly responsible for the delivery of timely trials wit...
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Posted Fri 10th May
The Clinical Research Nurse assists principal investigators in the development and implementation of clinical research for a specified study or project. Duties include: assisting with development of research protocols, assessing patients' condition, readiness and eligibility for study enrollment as a research subject and assisting in the preparation of research reports and statistical interpretati...
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Posted Thu 16th May
The Public Health Institute (PHI) is an independent, nonprofit organization dedicated to promoting health, well-being and quality of life for people throughout California, across the nation and around the world. As one of the largest and most comprehensive public health organizations in the nation, we are at the forefront of research and innovations to improve the efficacy of public health statewi...
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Posted Fri 26th April
The job outlook for qualified nurses is very positive as in many geographical areas, there are many more available positions than nurses to fill them. Employment is expected to grow at a fast pace because the nursing industry is a large industry and many new jobs will be created in addition to filling the needs of already understaffed facilities. Nurses can pick of many different specializations or be general study nurses. Education will include a minimum of completion of a nursing program or bachelor's degree and also a passing grade on the state licensing examination.
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